The following data is part of a premarket notification filed by Amsino Intl., Inc. with the FDA for Amsure Enteral Delivery Pump Set With Spike.
| Device ID | K992719 |
| 510k Number | K992719 |
| Device Name: | AMSURE ENTERAL DELIVERY PUMP SET WITH SPIKE |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | AMSINO INTL., INC. 833 TOWNE CENTER DR. Pomona, CA 91767 |
| Contact | Richard Y Li |
| Correspondent | Richard Y Li AMSINO INTL., INC. 833 TOWNE CENTER DR. Pomona, CA 91767 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-12 |
| Decision Date | 2000-01-12 |